Laurent M, Fleury A
Service d'Imagerie Cellulaire, URA 1116 CNRS, Université Paris-Sud, Orsay, France.
FEBS Lett. 1993 Dec 20;336(1):1-7. doi: 10.1016/0014-5793(93)81597-s.
In many cases, post-translational modifications constitute indirect markers of non-dynamic microtubules. The correlation between stability of microtubular systems and post-translational modifications suggests that they may act as a signal in patterning mechanisms. However, a crucial question remains as to how the repertoire of distinctly modified microtubules is generated. We propose here an ubiquitous mechanism of spatial and temporal differentiation of microtubules. In this model, the diversity of post-translational modifications results from a dynamical pathway separation which is ensured by biochemical switches between self-regulated mechanisms of differentiation. Thus, it does not require any hypothetical subcellular compartmentalization of enzymatic activities responsible for the various post-translational modifications. These results are discussed in relation to experimental evidences for a temporal and spatial regulation of microtubule modifications.
在许多情况下,翻译后修饰构成了非动态微管的间接标记。微管系统稳定性与翻译后修饰之间的相关性表明,它们可能在模式形成机制中充当信号。然而,一个关键问题仍然存在,即如何产生经过不同修饰的微管库。我们在此提出一种普遍存在的微管时空分化机制。在这个模型中,翻译后修饰的多样性源于动态途径分离,这是由分化的自我调节机制之间的生化开关确保的。因此,它不需要任何负责各种翻译后修饰的酶活性的假设性亚细胞区室化。结合微管修饰的时空调节的实验证据对这些结果进行了讨论。